Sokoine University of Agriculture

E2f8 mediates tumor suppression in postnatal liver development

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dc.contributor.author Machiraju, Raghu
dc.contributor.author Kent, L. N.
dc.contributor.author Rakijas, J. B.
dc.contributor.author Pandit, S. K.
dc.contributor.author Westendorp, B.
dc.contributor.author Chen, H.
dc.contributor.author Huntington, J. T.
dc.contributor.author Tang, X.
dc.contributor.author Bae, S.
dc.contributor.author Srivastava, A.
dc.contributor.author Senapati, S.
dc.contributor.author Koivisto, C.
dc.contributor.author Martin, C. K.
dc.contributor.author Cuitino, M. C.
dc.contributor.author Perez, M.
dc.contributor.author Matondo, R. B.
dc.date.accessioned 2018-10-05T07:34:34Z
dc.date.available 2018-10-05T07:34:34Z
dc.date.issued 2016-08-01
dc.identifier.uri https://www.jci.org/articles/view/85506
dc.identifier.uri http://www.suaire.sua.ac.tz/handle/123456789/2608
dc.description Endocrinology, 2009, 150 (1): 540-545 en_US
dc.description.abstract E2F-mediated transcriptional repression of cell cycle–dependent gene expression is critical for the control of cellular proliferation, survival, and development. E2F signaling also interacts with transcriptional programs that are downstream of genetic predictors for cancer development, including hepatocellular carcinoma (HCC). Here, we evaluated the function of the atypical repressor genes E2f7 and E2f8 in adult liver physiology. Using several loss-of-function alleles in mice, we determined that combined deletion of E2f7 and E2f8 in hepatocytes leads to HCC. Temporal-specific ablation strategies revealed that E2f8’s tumor suppressor role is critical during the first 2 weeks of life, which correspond to a highly proliferative stage of postnatal liver development. Disruption of E2F8’s DNA binding activity phenocopied the effects of an E2f8 null allele and led to HCC. Finally, a profile of chromatin occupancy and gene expression in young and tumor-bearing mice identified a set of shared targets for E2F7 and E2F8 whose increased expression during early postnatal liver development is associated with HCC progression in mice. Increased expression of E2F8-specific target genes was also observed in human liver biopsies from HCC patients compared to healthy patients. In summary, these studies suggest that E2F8-mediated transcriptional repression is a critical tumor suppressor mechanism during postnatal liver development en_US
dc.description.sponsorship NFP grant : R.B.M., DU.282001.1.3 en_US
dc.publisher The American Society for Clinical Investigation en_US
dc.subject Liver en_US
dc.subject E2f8 en_US
dc.subject Tumor en_US
dc.subject E2f en_US
dc.subject HCC en_US
dc.subject Hepatocyte en_US
dc.title E2f8 mediates tumor suppression in postnatal liver development en_US
dc.type Article en_US
dc.url https://www.jci.org/articles/view/85506 en_US


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